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British Journal of Haematology|April 1, 1993
The beta + IVS, I-NT no. 6 (T --> C) thalassaemia in heterozygotes with an associated Hb Valletta or Hb S heterozygosity in homozygotes from MaltaC A Scerri, W Abela, R Galdies, et al.Hemoglobin|January 1, 1978
Delta beta-thalassemia in a Mexican family: clinical differences among homozygotesG R Reyes, A Piña-Camara, A E Felice, et al.American Journal of Hematology|January 1, 1981
In vitro synthesis of hemoglobin and hemoglobin chains in the BFUe-derived colonies form person with alpha- or beta-thalassemiaT H Huisman, A L Reese, B Webber, et al.Pediatric Research|March 1, 1980
Hb S, Hb G-Philadelphia and alpha-thalassemia-2 in a Black familyA E Felice, S M Mayson, B B Webber, et al.Hemoglobin|January 1, 1980
Adult and fetal hemoglobin production in erythroid colonies from subjects with beta-thalassemia or with hereditary persistance of fetal hemoglobin (HPFH)T H Huisman, A L Reese, M E Gravely, et al.American Journal of Hematology|August 1, 1987
Effects of alpha-thalassemia-2 on the developmental changes of hematological values in children with sickle cell disease from GeorgiaA E Felice, K M McKie, M P Cleek, et al.British Journal of Haematology|February 1, 1985
(A gamma delta beta)0-Thalassaemia in Blacks is due to a deletion of 34 kbp of DNAP S Henthorn, O Smithies, T Nakatsuji, et al.The Journal of Laboratory and Clinical Medicine|June 1, 1979
Hb P-Nilotic in association with beta0-thalassemia: cis-mutation of a hemoglobin betaA chain regulatory determinant?A Abu-Sin, A E Felice, M E Gravely, et al.Human Genetics|July 1, 1986
Different zeta globin gene deletions among black AmericansA E Felice, M P Cleek, E M Marino, et al.Hemoglobin|January 1, 1989
Hb Evans or alpha 262(E11)Val----Met beta 2; an unstable hemoglobin causing a mild hemolytic anemiaJ B Wilson, B B Webber, A Kutlar, et al.Pageof 3